Evidence map›Paper›PMID 37166351›Full record

ReviewHuman molecular genetics2023

Epigenotype-genotype-phenotype correlations in SETD1A and SETD2 chromatin disorders.

Sunwoo Lee, Lara Menzies, Eleanor Hay, Eguzkine Ochoa, France Docquier, Fay Rodger, Charu Deshpande, Nicola C Foulds, Sébastien Jacquemont, Khadije Jizi and 13 more

Open access · hybridAbstract readReview
In one paragraph

Review in Human molecular genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. FamilialGenes · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Case report:Frontiers in neurology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 14 institutions in 5 countries.

Sunwoo LeeDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
Lara MenziesDepartment of Clinical Genetics, Great Ormond Street Hospital, London WC1N 3JH, UK.
Eleanor HayDepartment of Clinical Genetics, Great Ormond Street Hospital, London WC1N 3JH, UK.
Eguzkine OchoaDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
France DocquierDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
Fay RodgerDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
Charu DeshpandeManchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Saint Mary's Hospital, Manchester, UK.
Nicola C FouldsWessex Clinical Genetics Services, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Sébastien JacquemontCHU Sainte-Justine Research Centre, Montreal, Quebec, Canada.
Khadije JiziCHU Sainte-Justine Research Centre, Montreal, Quebec, Canada.
Henriette KiepDepartment of Neuropediatrics, University Hospital for Children and Adolescents, Leipzig, Germany.
Alison KrausYorkshire Regional Genetics Service, Chapel Allerton Hospital, Leeds, UK.
Katharina LöhnerDepartment of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Patrick J MorrisonPatrick G Johnston Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast, UK.
Bernt PoppInstitute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.
Ruth RichardsonNorthern Genetics Service, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
Arie van HaeringenDepartment of Clinical Genetics, Leiden University Hospital, Leiden, The Netherlands.
Ezequiel MartinDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
Ana ToribioDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.
Fudong LiMOE Key Laboratory for Cellular Dynamics, The School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230026, China.
Wendy D JonesDepartment of Clinical Genetics, Great Ormond Street Hospital, London WC1N 3JH, UK.
Francis H SansburyAll Wales Medical Genomics Service, NHS Wales Cardiff and Vale University Health Board and Institute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff, UK.ORCID 0000-0002-5048-3309
Eamonn R MaherDepartment of Medical Genetics, University of Cambridge, Cambridge CB2 0QQ, UK.ORCID 0000-0002-6226-6918
University of Cambridge · GBGreat Ormond Street Hospital · GBCentre Hospitalier Universitaire Sainte-Justine · CABerlin Institute of Health at Charité - Universitätsmedizin Berlin · DECardiff and Vale University Health Board · GBChapel Allerton Hospital · GBLeiden University · NLManchester University NHS Foundation Trust · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBQueen's University Belfast · GBUniversity Hospital Leipzig · DEUniversity Hospital Southampton NHS Foundation Trust · GBUniversity Medical Center Groningen · NLUniversity of Science and Technology of China · CN

Funding

Department of Health BRC-1215-20014Department of Health NIHR203312
6 · The paper itself

Abstract

Germline pathogenic variants in two genes encoding the lysine-specific histone methyltransferase genes SETD1A and SETD2 are associated with neurodevelopmental disorders (NDDs) characterized by developmental delay and congenital anomalies. The SETD1A and SETD2 gene products play a critical role in chromatin-mediated regulation of gene expression. Specific methylation episignatures have been detected for a range of chromatin gene-related NDDs and have impacted clinical practice by improving the interpretation of variant pathogenicity. To investigate if SETD1A and/or SETD2-related NDDs are associated with a detectable episignature, we undertook targeted genome-wide methylation profiling of > 2 M CpGs using a next-generation sequencing-based assay. A comparison of methylation profiles in patients with SETD1A variants (n = 6) did not reveal evidence of a strong methylation episignature. A review of the clinical and genetic features of the SETD2 patient group revealed that, as reported previously, there were phenotypic differences between patients with truncating mutations (n = 4, Luscan-Lumish syndrome; MIM:616831) and those with missense codon 1740 variants [p.Arg1740Trp (n = 4) and p.Arg1740Gln (n = 2)]. Both SETD2 subgroups demonstrated a methylation episignature, which was characterized by hypomethylation and hypermethylation events, respectively. Within the codon 1740 subgroup, both the methylation changes and clinical phenotype were more severe in those with p.Arg1740Trp variants. We also noted that two of 10 cases with a SETD2-NDD had developed a neoplasm. These findings reveal novel epigenotype-genotype-phenotype correlations in SETD2-NDDs and predict a gain-of-function mechanism for SETD2 codon 1740 pathogenic variants.

Indexed as

ChromatinNeurodevelopmental DisordersCodonDNA MethylationGenetic Association StudiesHumansMutationChromatinCodon

Identifiers

PMID37166351
PMCPMC10630252
OpenAlexW4376133537

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.